Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 20197-87-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloroquinazolin-4(1H)-one features a rigid, electron-deficient quinazoline core with strategically positioned chlorine substituents. This configuration enhances its utility as a synthetic intermediate in medicinal chemistry, particularly for constructing kinase inhibitors and bioactive heterocycles under standard coupling conditions.
2,6-Dichloroquinazolin-4(1H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted quinazoline scaffolds through nucleophilic displacement and palladium-catalyzed coupling reactions. Its dichloro substitution pattern provides orthogonal reactivity for sequential functionalization, while the quinazolinone core exhibits bench stability and compatibility with common purification methods. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive heterocycles.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: